Canonical Allele Identifier: CA349407175

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179395307T>A (hg19) ; chr2:g.178530580T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178530580T>A , CM000664.2:g.178530580T>A	GRCh38
NC_000002.11:g.179395307T>A , CM000664.1:g.179395307T>A	GRCh37
NC_000002.10:g.179103553T>A	NCBI36
NG_011618.3:g.305223A>T , LRG_391:g.305223A>T
NG_051363.1:g.12754T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.98331A>T (TTN)	ENSP00000343764.6:p.Lys32777Asn
ENST00000342175.11:c.79416A>T (TTN)	ENSP00000340554.6:p.Lys26472Asn
ENST00000359218.10:c.79215A>T (TTN)	ENSP00000352154.5:p.Lys26405Asn
ENST00000342175.10:c.79416A>T (TTN)	ENSP00000340554.6:p.Lys26472Asn
ENST00000342992.10:c.98331A>T (TTN)	ENSP00000343764.6:p.Lys32777Asn
ENST00000359218.9:c.79215A>T (TTN)	ENSP00000352154.5:p.Lys26405Asn
ENST00000460472.6:c.78840A>T (TTN)	ENSP00000434586.1:p.Lys26280Asn
ENST00000589042.5:c.106035A>T (TTN) MANE Select	ENSP00000467141.1:p.Lys35345Asn
ENST00000591111.5:c.101112A>T (TTN)	ENSP00000465570.1:p.Lys33704Asn
ENST00000615779.4:c.101112A>T (TTN)	ENSP00000483597.1:p.Lys33704Asn
NM_001256850.1:c.101112A>T (TTN)	NP_001243779.1:p.Lys33704Asn
NM_001267550.2:c.106035A>T (TTN) MANE Select	NP_001254479.2:p.Lys35345Asn
NM_003319.4:c.78840A>T (TTN)	NP_003310.4:p.Lys26280Asn
NM_133378.4:c.98331A>T (TTN)	NP_596869.4:p.Lys32777Asn
NM_133432.3:c.79215A>T (TTN)	NP_597676.3:p.Lys26405Asn
NM_133437.4:c.79416A>T (TTN)	NP_597681.4:p.Lys26472Asn
NR_038271.1:n.446+6944T>A (TTN-AS1)
NR_038272.1:n.220-5152T>A (TTN-AS1)
XM_011511729.1:c.105132A>T (TTN)	XP_011510031.1:p.Lys35044Asn
XM_011511730.1:c.79026A>T (TTN)	XP_011510032.1:p.Lys26342Asn
XM_011511731.1:c.78885A>T (TTN)	XP_011510033.1:p.Lys26295Asn
XM_017004819.1:c.104928A>T (TTN)	XP_016860308.1:p.Lys34976Asn
XM_017004820.1:c.100326A>T (TTN)	XP_016860309.1:p.Lys33442Asn
XM_017004821.1:c.100323A>T (TTN)	XP_016860310.1:p.Lys33441Asn
XM_017004822.1:c.97365A>T (TTN)	XP_016860311.1:p.Lys32455Asn
XM_017004823.1:c.78981A>T (TTN)	XP_016860312.1:p.Lys26327Asn
XM_024453094.1:c.100476A>T (TTN)	XP_024308862.1:p.Lys33492Asn
XM_024453095.1:c.100473A>T (TTN)	XP_024308863.1:p.Lys33491Asn
XM_024453096.1:c.99906A>T (TTN)	XP_024308864.1:p.Lys33302Asn
XM_024453097.1:c.97248A>T (TTN)	XP_024308865.1:p.Lys32416Asn
XM_024453098.1:c.97167A>T (TTN)	XP_024308866.1:p.Lys32389Asn
XM_024453099.1:c.78930A>T (TTN)	XP_024308867.1:p.Lys26310Asn
XM_024453100.1:c.68784A>T (TTN)	XP_024308868.1:p.Lys22928Asn